Spectrum of Genetic Changes in Patients with Non-Syndromic Hearing Impairment and Extremely High Carrier Frequency of 35delG GJB2 Mutation in Belarus

Open Access

Peer-reviewed

Research Article

Nina Danilenko ,

* E-mail: n.danilenko@tut.by

Affiliation Institute of Genetics and Cytology, National Academy of Sciences, Minsk, Belarus
⨯
Elena Merkulava,

Affiliation Belarusian State Medical University, Minsk, Belarus
⨯
Marina Siniauskaya,

Affiliation Institute of Genetics and Cytology, National Academy of Sciences, Minsk, Belarus
⨯
Olga Olejnik,

Affiliation Institute of Genetics and Cytology, National Academy of Sciences, Minsk, Belarus
⨯
Anastasia Levaya-Smaliak,

Affiliation Belarusian State Medical University, Minsk, Belarus
⨯
Alena Kushniarevich,

Affiliation Estonian Biocentre, Tartu, Estonia
⨯
Andrey Shymkevich,

Affiliation Institute of Genetics and Cytology, National Academy of Sciences, Minsk, Belarus
⨯
Oleg Davydenko

Affiliation Institute of Genetics and Cytology, National Academy of Sciences, Minsk, Belarus
⨯

Reader Comments (0)

Belarus
Is the Subject Area "Belarus" applicable to this article?

Thanks for your feedback.
Deafness
Is the Subject Area "Deafness" applicable to this article?

Thanks for your feedback.
Mitochondria
Is the Subject Area "Mitochondria" applicable to this article?

Thanks for your feedback.
Point mutation
Is the Subject Area "Point mutation" applicable to this article?

Thanks for your feedback.
Substitution mutation
Is the Subject Area "Substitution mutation" applicable to this article?

Thanks for your feedback.
Belarusian people
Is the Subject Area "Belarusian people" applicable to this article?

Thanks for your feedback.
Deletion mutation
Is the Subject Area "Deletion mutation" applicable to this article?

Thanks for your feedback.
Carrier frequencies
Is the Subject Area "Carrier frequencies" applicable to this article?

Thanks for your feedback.